ClinVar Miner

List of variants in gene ZFYVE26 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.7417-5G>C rs201771769 0.00236
NM_015346.4(ZFYVE26):c.773G>A (p.Arg258Gln) rs150230201 0.00113
NM_015346.4(ZFYVE26):c.1945G>A (p.Val649Met) rs144790966 0.00107
NM_015346.4(ZFYVE26):c.5260G>A (p.Ala1754Thr) rs146968463 0.00045
NM_015346.4(ZFYVE26):c.2396C>T (p.Thr799Met) rs200179480 0.00014
NM_015346.4(ZFYVE26):c.5321-3C>T rs376234357 0.00011
NM_015346.4(ZFYVE26):c.5767C>T (p.Arg1923Trp) rs544932478 0.00009
NM_015346.4(ZFYVE26):c.730C>A (p.Leu244Ile) rs148790248 0.00009
NM_015346.4(ZFYVE26):c.5768G>A (p.Arg1923Gln) rs199497582 0.00006
NM_015346.4(ZFYVE26):c.403G>A (p.Val135Met) rs771937001 0.00003
NM_015346.4(ZFYVE26):c.6973G>A (p.Ala2325Thr) rs763267244 0.00002
NM_015346.4(ZFYVE26):c.1153A>T (p.Arg385Trp) rs529988015 0.00001
NM_015346.4(ZFYVE26):c.1170G>A (p.Leu390=) rs532292359 0.00001
NM_015346.4(ZFYVE26):c.295C>T (p.Arg99Trp) rs779962087 0.00001
NM_015346.4(ZFYVE26):c.6870A>G (p.Ser2290=) rs766701632 0.00001
NM_015346.4(ZFYVE26):c.1073T>C (p.Leu358Pro) rs2040164683
NM_015346.4(ZFYVE26):c.175G>T (p.Val59Leu) rs1555401096
NM_015346.4(ZFYVE26):c.2498C>T (p.Pro833Leu)
NM_015346.4(ZFYVE26):c.2614C>T (p.Arg872Cys)
NM_015346.4(ZFYVE26):c.2993G>A (p.Arg998His)
NM_015346.4(ZFYVE26):c.3097A>T (p.Ser1033Cys) rs1555397623
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.3806C>T (p.Pro1269Leu) rs2140223671
NM_015346.4(ZFYVE26):c.3811T>C (p.Ser1271Pro) rs2039558721
NM_015346.4(ZFYVE26):c.4408G>A (p.Asp1470Asn) rs1388977274
NM_015346.4(ZFYVE26):c.4525T>C (p.Cys1509Arg) rs1594911188
NM_015346.4(ZFYVE26):c.5402C>G (p.Ala1801Gly)
NM_015346.4(ZFYVE26):c.5510G>A (p.Arg1837His) rs776920735
NM_015346.4(ZFYVE26):c.5510G>C (p.Arg1837Pro) rs776920735
NM_015346.4(ZFYVE26):c.6008A>G (p.Asp2003Gly) rs890614624
NM_015346.4(ZFYVE26):c.715C>T (p.Leu239=)

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